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dc.contributor.authorBerners-Price, Sueen_US
dc.contributor.authorColquhoun, Lyndaen_US
dc.contributor.authorHealy, Peteren_US
dc.contributor.authorByriel, Karl A.en_US
dc.contributor.authorV. Hanna, Johnen_US
dc.date.accessioned2017-04-24T07:59:50Z
dc.date.available2017-04-24T07:59:50Z
dc.date.issued1992en_US
dc.date.modified2009-08-21T06:35:39Z
dc.identifier.issn14727773en_US
dc.identifier.doi10.1039/DT9920003357en_AU
dc.identifier.urihttp://hdl.handle.net/10072/19519
dc.description.abstractThe synthesis, structural and solid-state 31P cross-polarization magic angle spinning (CP MAS) NMR characterization of cis-bis(diphenylphosphino)ethylene (dppey) and the copper(I) and gold(I) complexes [M(dppey)2]PF6 has been carried out. The complexes, which have been shown to exhibit cytotoxic and antitumour activity, belong to the relatively rare class of copper(I) and gold(I) complexes with tetrahedral CuP4 and AuP4 co-ordination spheres. Crystals of dppey 1 are monoclinic with space group P21/c and a= 12.861(8), b= 13.097(2), c= 14.228(8)Ŭ = 116.15(3)໠R was 0.047 for 3117 observed reflections. The solid-state CP MAS 31P NMR spectrum consists of an AB multiplet with (PA)-24.2, (PB)-27.2 and J(P-P)= 126 Hz. Crystals of [Cu(dppey)2]PF62 are orthorhombic with space group P212121 and a= 14.479(5), b= 16.703(4), c= 20.891(4)Ż R was 0.046 for 3138 observed reflections. The CuP4 co-ordination sphere is regular within the constraints of chelation with Cu-P in the range 2.276(2)-2.289(2)Ů The copper atom lies on a pseudo two-fold axis of symmetry bisecting the CC bonds. Charge-transfer interactions between phenyl rings on each ligand contribute to the stabilization of the structure of the cation. The solid-state 31P NMR spectrum consists of four broad bands (�300 Hz) centred at 8 with J(Cu-P) 820 Hz. Distortion of the quartet spacings by quadrupolar interaction with the copper nuclei is minimal. Crystals of [Au(dppey)2]PF63 are isomorphous with 2 with a= 14.644(4), b= 16.703(1), c= 20.699(5)Ż R was 0.025 for 3947 observed reflections. The Au-P distances lie in the narrow range 2.377(2)-2.388(2)Ů Solid-state CP MAS 31P NMR of this complex and the analogous nitrate and chloride complexes at magnetic field strengths of 2.11, 7.05 and 9.40 T reveal splitting of the phosphorus signal into a quartet ascribed to Au-P spin-spin coupling effects with J(Au-P) estimated to be 200 Hz. As for the copper complex, distortion of the quartet spacings is minimal and indicative of a small 197Au quadrupolar coupling constant. Solution and solid-state 31P NMR chemical shift parameters are similar, supporting the hypothesis that the tetrahedral bis(chelated) cations are also stable in solution. Spin-spin coupling to the quadrupolar (197Au or 63/65Cu) nuclei was not resolved in the solution spectra, however, due to rapid quadrupolar relaxation.en_US
dc.description.peerreviewedYesen_US
dc.description.publicationstatusYesen_AU
dc.languageEnglishen_US
dc.language.isoen_AU
dc.publisherRoyal Society of Chemistryen_US
dc.publisher.placeUnited Kingdomen_US
dc.publisher.urihttp://www.rsc.org/Publishing/Journals/dt/en_AU
dc.relation.ispartofpagefrom3357en_US
dc.relation.ispartofpageto3363en_US
dc.relation.ispartofissue23en_US
dc.relation.ispartofjournalJournal of the Chemical Society, Dalton Transactionsen_US
dc.relation.ispartofvolume1992en_US
dc.subject.fieldofresearchcode250105en_US
dc.titleCopper(I) and gold(I) complexes with cis-bis(diphenylphosphino)ethylene. Crystal structures and 31P cross-polarization magic angle spinning nuclear magnetic resonance studies.en_US
dc.typeJournal articleen_US
dc.type.descriptionC1 - Peer Reviewed (HERDC)en_US
dc.type.codeC - Journal Articlesen_US
gro.facultyOffice of the Snr Dep Vice Chancellor, Institute for Glycomicsen_US
gro.rights.copyrightCopyright 1992 Royal Society of Chemistry. Please refer to the journal link for access to the definitive, published version.en_AU
gro.date.issued1992
gro.hasfulltextNo Full Text


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